Canonical Allele Identifier: CA379562826

Gene: TUB

Linked Data

• gnomAD v4: 11-8090139-G-C
• MyVariant Identifiers: chr11:g.8111686G>C (hg19) ; chr11:g.8090139G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.8090139G>C , CM000673.2:g.8090139G>C	GRCh38
NC_000011.9:g.8111686G>C , CM000673.1:g.8111686G>C	GRCh37
NC_000011.8:g.8068262G>C	NCBI36
NG_029912.1:g.56507G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299506.3:c.161G>C MANE Select	ENSP00000299506.3:p.Gly54Ala
ENST00000299506.2:c.161G>C	ENSP00000299506.2:p.Gly54Ala
ENST00000305253.8:c.326G>C	ENSP00000305426.4:p.Gly109Ala
ENST00000534099.5:c.179G>C	ENSP00000434400.1:p.Gly60Ala
NM_003320.4:c.326G>C	NP_003311.2:p.Gly109Ala
NM_177972.2:c.161G>C	NP_813977.1:p.Gly54Ala
XM_005253109.2:c.287G>C	XP_005253166.1:p.Gly96Ala
XM_011520344.1:c.197G>C	XP_011518646.1:p.Gly66Ala
XM_005253109.3:c.287G>C	XP_005253166.1:p.Gly96Ala
XM_011520344.2:c.197G>C	XP_011518646.1:p.Gly66Ala
NM_177972.3:c.161G>C MANE Select	NP_813977.1:p.Gly54Ala
NM_003320.5:c.326G>C	NP_003311.2:p.Gly109Ala